Hirschburger Daniela, Müller Manuel, Voegele Ralf T, Link Tobias
Department of Phytopathology, Institute of Phytomedicine, Faculty of Agricultural Sciences, University of Hohenheim, Otto-Sander-Straße 5, 70599 Stuttgart, Germany.
Int J Mol Sci. 2015 Sep 23;16(9):23057-75. doi: 10.3390/ijms160923057.
Phakopsora pachyrhizi is a devastating pathogen on soybean, endangering soybean production worldwide. Use of Host Induced Gene Silencing (HIGS) and the study of effector proteins could provide novel strategies for pathogen control. For both approaches quantification of transcript abundance by RT-qPCR is essential. Suitable stable reference genes for normalization are indispensable to obtain accurate RT-qPCR results. According to the Minimum Information for Publication of Quantitative Real-Time PCR Experiments (MIQE) guidelines and using algorithms geNorm and NormFinder we tested candidate reference genes from P. pachyrhizi and Glycine max for their suitability in normalization of transcript levels throughout the infection process. For P. pachyrhizi we recommend a combination of CytB and PDK or GAPDH for in planta experiments. Gene expression during in vitro stages and over the whole infection process was found to be highly unstable. Here, RPS14 and UbcE2 are ranked best by geNorm and NormFinder. Alternatively CytB that has the smallest Cq range (Cq: quantification cycle) could be used. We recommend specification of gene expression relative to the germ tube stage rather than to the resting urediospore stage. For studies omitting the resting spore and the appressorium stages a combination of Elf3 and RPS9, or PKD and GAPDH should be used. For normalization of soybean genes during rust infection Ukn2 and cons7 are recommended.
大豆锈病菌(Phakopsora pachyrhizi)是大豆上一种极具破坏力的病原菌,危及全球大豆生产。利用寄主诱导基因沉默(HIGS)和效应蛋白研究可为病原菌控制提供新策略。对于这两种方法,通过逆转录定量聚合酶链反应(RT-qPCR)对转录本丰度进行定量至关重要。合适的稳定内参基因对于获得准确的RT-qPCR结果不可或缺。根据《实时定量PCR实验发表的最低信息》(MIQE)指南,并使用geNorm和NormFinder算法,我们测试了来自大豆锈病菌和大豆(Glycine max)的候选内参基因在整个感染过程中用于转录水平标准化的适用性。对于大豆锈病菌,我们建议在植物体内实验中使用细胞色素B(CytB)和丙酮酸脱氢酶激酶(PDK)或甘油醛-3-磷酸脱氢酶(GAPDH)的组合。发现在体外阶段和整个感染过程中的基因表达高度不稳定。在此,核糖体蛋白S14(RPS14)和泛素结合酶E2(UbcE2)在geNorm和NormFinder中排名最佳。或者,可以使用Cq范围最小的CytB(Cq:定量循环)。我们建议将基因表达指定为相对于芽管阶段,而不是相对于静止的夏孢子阶段。对于省略静止孢子和附着胞阶段的研究,应使用Elf3和RPS9或PKD和GAPDH的组合。对于锈病感染期间大豆基因的标准化,建议使用Ukn2和cons7。